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VVI起搏治疗先天性长QT综合征12例随访

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摘要 先天性长QT综合征(Long QT Syndrome,LQ偈)是由于编码心脏离子通道的基因突变导致相应的离子通道功能异常而引起的一组综合征,主要表现为心律紊乱[1]。LQTS并非常见病,但该病发病突然、猝死率高、且以青少年发病多见。
出处 《心脑血管病防治》 2013年第3期232-233,共2页 CARDIO-CEREBROVASCULAR DISEASE PREVENTION AND TREATMENT
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参考文献5

  • 1Antzelevitch C. Lonic, molecular, and cellular bases of QT-interval pro- longation and torsade de pointes[ J ]. Ettropace, 2007,9 (suppl 4):4- 15.
  • 2Zipes DP, Cmmn AJ, Borggrefe M, et al. ACC/AHA/ESC 2006 guide- lines for management of patients with ventricular arrhythmias and the pre- vention of sudden cardiac death[J]. Europace,2006,8(9) :746 - 837.
  • 3Crotti L, Spazzolini C, Schwartz PJ, et al. The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification[J]. Circulation,2007,116(21 ) :2366 - 2375.
  • 4李翠兰,胡大一,王吉云,刘文玲,梅运清,商利华,马山,马志敏.左心交感神经切除术治疗长QT综合征11例随访[J].中国心脏起搏与心电生理杂志,2006,20(1):21-24. 被引量:12
  • 5孙奇,陈柯萍,陈若菡,华伟,浦介麟,张澍.植入型心律转复除颤器在长QT综合征患者中的应用[J].中华心律失常学杂志,2008,12(5):342-344. 被引量:3

二级参考文献19

  • 1薛小临,廉姜芳,崔长琮.长QT综合征的治疗进展[J].中华心律失常学杂志,2005,9(5):395-398. 被引量:6
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